Examples of 'aluminum hydride' in a sentence
Meaning of "aluminum hydride"
aluminum hydride: This phrase is a chemical term referring to a compound composed of aluminum and hydrogen. It is commonly used in various chemical reactions, including reductions and organic synthesis
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- Alternative spelling of aluminium hydride
How to use "aluminum hydride" in a sentence
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aluminum hydride
Reduction with lithium aluminum hydride is preferred.
Aluminum hydride may replace borohydride.
The preferred reagent is lithium aluminum hydride.
Lithium aluminum hydride is particularly preferred.
An example of reducing agent is lithium aluminum hydride.
Diisobutyl aluminum hydride is particularly preferred.
A suitable reducing agent is lithium aluminum hydride.
Lithium aluminum hydride is the preferred reducing agent.
The reducing agent is advantageously lithium aluminum hydride.
Lithium aluminum hydride is prefectly suitable to promote such a reaction.
Tetrahydrofuran was dried by distillation over lithium aluminum hydride.
Trimethoxy aluminum hydride is preferable.
Preferably the reducing agent is lithium aluminum hydride.
Lithium aluminum hydride can be used as the reducing agent.
Purchase lithium aluminum hydride.
See also
Lithium aluminum hydride can also be used by itself as a solid fuel.
The borane was added to this alkoxy aluminum hydride vÃa syringe.
Excess lithium aluminum hydride was carefully quenched with water.
From the acid derivatives by reduction with lithium aluminum hydride.
Lithium aluminum hydride and diborane are used as the reducing agent.
These reduction conditions provide an alternative to a lithium aluminum hydride reduction.
Lithium aluminum hydride and tetrahydrofuran is the preferred reaction medium.
Ethyl ether was distilled from lithium aluminum hydride prior to use.
Lithium aluminum hydride reduction of alkyl substituted isoxazoles gave a variety of products.
The reducing agent employed here is preferably diisobutyl aluminum hydride.
Lithium aluminum hydride is the preferred reducing agent for the process.
Preferred metal hydrides are lithium aluminum hydride and aluminum hydride.
Lithium aluminum hydride is illustrated in the synthetic example set forth below.
Also reducing agent such as lithium aluminum hydride can be used.
Excess lithium aluminum hydride was neutralized with a saturated ammonium chloride solution.
The cyclic peptide is then reduced with lithium aluminum hydride.
Lithium aluminum hydride is the preferred reducing agent for this reaction.
The ester was further reduced to alcohol using lithium aluminum hydride.
Lithium aluminum hydride and sodium borohydride are representative examples of suitable reducing agents.
The resulting cyclic triamide is then reduced with lithium aluminum hydride.
Excess lithium aluminum hydride is quenched with portions of ethyl acetate followed by water.
This derivative is then reduced and detosylated with lithium aluminum hydride.
Lithium aluminum hydride in an ether solvent such as tetrahydrofuran is preferred for this conversion.
The reducing agent may be a known reducing agent such as lithium aluminum hydride.
Lithium aluminum hydride and tetrahydrofuran are the preferred solvent and reducing agent.
Preferred metal hydride reducing agents include lithium aluminum hydride or sodium cyanoborohydride.
Lithium aluminum hydride is preferred for the formation of compounds of formula XIII.
This mixture is then contacted with a reducing agents such as diisobutyl aluminum hydride.
Reduction of the amide with lithium aluminum hydride provides final cationic lipids viii.
The resulting macrocyclic diamide is reduced and detosylated with lithium aluminum hydride.
Examples of the metal hydride compound include aluminum hydride compounds and boron hydride compounds.
The resulting cyclic amide is then reduced and detosylated with lithium aluminum hydride.
This reduction may be carried out using lithium aluminum hydride or other strong reducing agent.
Examples of the reagent used include general reducing agents such as lithium aluminum hydride.
Amide xiii can be reduced with lithium aluminum hydride in THF to afford aldehyde xiv.
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Examples of using Hydride
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Using on a nickel metal hydride rechargeable battery
Sodium hydride or sodium amide is preferably used
The preferred metal hydride is sodium hydride
Examples of using Aluminum
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Aluminum reflector is standard for all versions
Bench wise with aluminum soft jaws
Mix aluminum powder with iron oxide
